Solubility enhancing peptide and use thereof

Abstract

The present invention relates to an isolated peptide consisting of the amino acid sequence of SEQ ID NO: 1. The present invention also relates to a method for increasing expression of a target protein using the peptide consisting of the amino acid sequence of SEQ ID NO: 1, comprising (a) fusing the peptide with the target protein to form a recombinant protein; and (b) expressing the recombinant protein by an expression host.

Description

CROSS-REFERENCES TO RELATED APPLICATIONS

The present application is a regular application which claims priority to U.S. Provisional Application No. 61/823,531, filed on May 15, 2013, incorporated herein by reference in its entirety.

FIELD OF THE INVENTION

The present invention relates to an artificial peptide and use thereof.

The sequence listing text file, file name 2298_NTHU_SQlist_ST25, created May 9, 2014, file size 17,869 bytes, is incorporated herein by reference in its entirety.

BACKGROUND OF THE INVENTION

The supply of many valuable proteins that have potential clinical or industrial use is often limited by their low natural availability. With the modern advances in genomics, proteomics and bioinformatics, the number of proteins being produced using recombinant techniques is exponentially increasing and seems to guarantee an unlimited supply of recombinant proteins. However, the soluble expression of heterologous proteins in E. coli remains a serious bottleneck in protein production. Overexpression of cloned genes in E. coli may lead to the formation of intracellular proteinaceous granules that are readily visible under the light microscope. A number of parameters relating to the host cell, the growth conditions and the properties of the particular protein affect this process. Therefore, new technologies to enhance protein expression and simplify the purification process are needed to help protein investigation at the scale of many proteins simultaneously.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows purification and characterization of recombinant bacteria recognizing lectin (rBRL). After induction with 0.1 mM IPTG at 16° C. for 16 h, the supernatant of cell lysate containing rBRL is collected by centrifugation and subjected to Nickel column chromatography for purification. Aliquots of each fraction are analyzed by 15% (w/v) SDS-PAGE. Lane M: molecular weight marker; Lane N: cell lysate of E. coli without IPTG induction; Lane I: cell lysate of E. coli with IPTG induction; Lane P: insoluble pellet; Lane S: supernatant; Lane F: binding flow-through; Lane W1: washing fraction with 20 mM Tris-HCl, 200 mM NaCl, 5 mM imidazole; Lane W2: washing fraction with 20 mM Tris-HCl, 200 mM NaCl, 50 mM imidazole; Lane E: eluting fraction with 20 mM Tris-HCl, 200 mM NaCl, 300 mM imidazole; Lane C: concentrated fraction.

FIG. 2 shows small-scale expression of rBRL (N7) and rBRL (C7). Expression of (A) rBRL (N7) and (B) rBRL (C7) are induced by addition of 0.1 mM IPTG to the cultures and incubation at 16° C. for 16 h. Twenty microliters sample of each fraction is separated by 15% (w/v) SDS-PAGE and stained with Coomassie blue. Lane M: molecular weight marker; Lane N: cell lysate of E. coli without IPTG induction; Lane I: cell lysate of E. coli with IPTG induction; Lane P: insoluble pellet; Lane S: supernatant.

FIG. 3A shows purification and characterization of recombinant human eosinophil ribonuclease (reRNase). After induction with 0.1 mM IPTG at 16° C. for 16 h, the supernatant of cell lysate containing reRNase is collected by centrifugation and subjected to Heparin column chromatography for purification. Aliquots of each fraction are analyzed by 15% (w/v) SDS-PAGE. Lane M: molecular weight marker; Lane N: cell lysate of E. coli without IPTG induction; Lane I: cell lysate of E. coli with IPTG induction; Lane P: insoluble pellet; Lane S: supernatant; Lane F: binding flow-through; Lane W: washing fraction with 10 mM sodium phosphate buffer, 1 mM EDTA, E1˜E4: eluting fraction with 10 mM sodium phosphate buffer, 1 mM EDTA, 0-2M NaCl. FIG. 3B shows small-scale expression of RNase 3. Without an artificial peptide, reRNase major present in insoluble pellet after induction with 0.1 mM IPTG at 16° C. for 16 h.

FIG. 4 shows primary sequence alignment of six kinds of mature eosinophil RNase sequences originated from different primates, including Homo sapiens, Pantroglodytes, Gorilla Gorilla, Macaca fascicularis, Macaca nemestrina, and Pongo pygmaeus. Primate eosinophil RNase sequences were extracted from NCBI database. Sequences are aligned using Clustal X2. Fully conserved amino acids are indicated by asterisk (*), highly similar amino acids are indicated by colon (:), and weakly similar amino acids are indicated by dot (.). eRNase_HUMAN means human eosinophil RNase (SEQ ID NO: 9); eRNase_PANTR means Pan troglodytes eosinophil RNase (SEQ ID NO: 14); eRNase_GORGO means Gorilla Gorilla eosinophil RNase (SEQ ID NO: 15); eRNase_MACFA means Macaca fascicularis eosinophil RNase (SEQ ID NO: 16); eRNase_MACNE means Macaca nemestrina eosinophil RNase (SEQ ID NO: 17); and eRNase_PONPY means Pongo pygmaeus eosinophil RNase (SEQ ID NO: 18).

SUMMARY OF THE INVENTION

The present invention relates to an isolated peptide consisting of the amino acid sequence of SEQ ID NO: 1. The present invention also relates to a method for increasing expression of a target protein by using the peptide consisting of the amino acid sequence of SEQ ID NO: 1, comprising (a) fusing the peptide with the target protein to form a recombinant protein; and (b) expressing the recombinant protein by an expression host.

DETAILED DESCRIPTION OF THE INVENTION

Fusion protein approach may overcome the low expression obstacle using affinity tags for increasing protein expression, and aiding in protein purification efficiency.

An artificial peptide was designed to increase solubility of a target fusion protein. An example of the amino acid sequence of such artificial peptide includes but is not limited to SKPTTTTTTTTTAPSTSTTTRPSSSEPATFPTGDSTISS (SEQ ID NO: 1).

Horseshoe crab bacteria recognizing lectin (BRL) derived from hemocyte of Taiwanese Tachypleus tridentatus is a LPS-binding protein isolated from plasma. An example of the amino acid sequence of BRL includes but is not limited to

(SEQ ID NO: 2)
EDDCTCVTDRSLEGKLMKHPSTPAVYQILDGCRRLVPNPPTYNNIYKNW
ECIQSNILEKLLCKCDSLSNGAELIKGSGDTVYLLSNGVKRPIADPETF
NGFCFDWNKIKTYSDIVINSLSTGPIIIIK.

Human eosinophil ribonuclease (RNase) belongs to RNase A superfamily and is secreted by eosinophil during inflammation. Primate eosinophil RNase sequences were extracted from NCBI database and aligned with human eosinophil RNase (FIG. 4). Human eosinophil RNase shows high degree of similarity to primate eosinophil RNases (higher than 86% sequence identity). Human eosinophil RNase is composed of 133 amino acids with isoelectricpoint of 10.8. An example of the amino acid sequence of human eosinophil RNase includes but is not limited to

(SEQ ID NO: 9)
RPPQFTRAQWFAIQHISLNPPRCTIAMRAINNYRWRCKNQNTFLRTTFA
NVVNVCGNQSIRCPHNRTLNNCHRSRFRVPLLHCDLINPGAQNISNCTY
ADRPGRRFYVVACDNRDPRDSPRYPVVPVHLDTTI.

In this invention, a novel recombinant protein rBRL comprising an N-terminal 39-amino acid artificial peptide and a C-terminal 128-amino acid BRL, (for example: MSKPTTTTTTTTTAPSTSTTTRPSSSEPATFPTGDSTISSEFEDDCTCVTDRSLEG KLMKHPSTPAVYQILDGCRRLVPNPPTYNNIYKNWECIQSNILEKLLCKCDSLS NGAELIKGSGDTVYLLSNGVKRPIADPETFNGFCFDWNKIKTYSDIVINSLSTG PIIIIKHHHHHH (SEQ ID NO: 3)), has been created in E. coli expression system. The 1^st amino acid residue (M) and the 41^th to 42^th amino acid residues (EF) of SEQ ID NO: 3 are residues derived from vector pET23a and may be altered when different vector is used, even can be absent in one aspect of the present invention. In addition, the 6 residues at the end of SEQ ID NO: 3 (HHHHHH) functions as a tag for purification and can be replaced by any other sequence having similar function, even can be absent in one aspect of the present invention. According the above, it is noted that the present invention also provides a kind of rBRL which consists of the amino acid sequence of SEQ ID NO: 4 (SKPTTTTTTTTTAPSTSTTTRPSSSEPATFPTGDSTISSEDDCTCVTDRSLEGKL MKHPSTPAVYQILDGCRRLVPNPPTYNNIYKNWECIQSNILEKLLCKCDSLSNG AELIKGSGDTVYLLSNGVKRPIADPETFNGFCFDWNKIKTYSDIVINSLSTGPIII IK).

In this study, a novel recombinant protein recombinant eosinophil ribonuclease (reRNase) comprising an N-terminal 39-amino acid artificial peptide and a C-terminal 133-amino acid human eosinophil RNase, (for example: MSKPTTTTTTTTTAPSTSTTTRPSSSEPATFPTGDSTISSEFRPPQFTRAQWFAIQ HISLNPPRCTIAMRAINNYRWRCKNQNTFLRTTFANVVNVCGNQSIRCPHNRT LNNCHRSRFRVPLLHCDLINPGAQNISNCTYADRPGRRFYVVACDNRDPRDS PRYPVVPVHLDTTIHHHHHH (SEQ ID NO: 10)), has been created in E. coli expression system. The 1^st amino acid residue (M) and the 41^th to 42^th amino acid residues (EF) of SEQ ID NO: 10 are residues derived from vector pET23a and may be altered when different vector is used, even can be absent in one aspect of the present invention. In addition, the 6 residues at the end of SEQ ID NO: 10 (HHHHHH) functions as a tag for purification and can be replaced by any other sequence having similar function, even can be absent in one aspect of the present invention. According the above, it is noted that the present invention also provides a kind of reRNase which consists of the amino acid sequence of SEQ ID NO: 11 (SKPTTTTTTTTTAPSTSTTTRPSSSEPATFPTGDSTISSRPPQFTRAQWFAIQHIS LNPPRCTIAMRAINNYRWRCKNQNTFLRTTFANVVNVCGNQSIRCPHNRTLN NCHRSRFRVPLLHCDLINPGAQNISNCTYADRPGRRFYVVACDNRDPRDSPR YPVVPVHLDTTI).

It is noted that any mutation of the above amino acid sequences with the similar activities is involved in the scope of the present invention.

Addition of the artificial peptide (SEQ ID NO: 1) successfully enhances BRL or eosinophil RNase expression as well as simplifies the purification process.

The terms used in the description herein will have their ordinary and common meaning as understood by those skilled in the art, unless specifically defined otherwise.

Thus, the present invention provides an isolated peptide consisting of the amino acid sequence of SEQ ID NO: 1. The present invention also provides a method for increasing expression of a target protein by using an isolated peptide consisting of the amino acid sequence of SEQ ID NO: 1, comprising (a) fusing the peptide with the target protein to form a recombinant protein; and (b) expressing the recombinant protein by an expression host. Preferably, the target protein is a glycan binding protein; more preferably, the target protein is a vertebrate plasma lectin or a vertebrate ribonuclease; still more preferably, the target protein is a bacteria recognizing lectin or a primate eosinophil ribonuclease; still more preferably, the target protein is a human eosinophil ribonuclease. In an embodiment, the expression host is a bacterium, a yeast, an insect cell or a mammalian cell. More preferably, the bacterium is Escherichia coli. The method not only simplifies the purification process for the target protein but also retains activity of the target protein after fusing the peptide to the target protein.

EXAMPLES

The examples below are non-limiting and are merely representative of various aspects and features of the present invention.

Example 1

Materials and Methods

Reagents

E. coli Top10F′ (Invitrogen) was used for vector construction and DNA manipulation, E. coli expression strain ROSETTA™ (DE3) (Stratagene), vectors pET23a purchased from NOVAGEN® were used for protein expression. All other buffers and reagents are of the highest commercial purity.

Protein Expression and Purification

DNA fragment encoding SEQ ID NO: 1 was amplified by PCR with primers 5′ NdeI-ANP (5′ CATATGTCCAAGCCACTACTACTAC 3′) (SEQ ID NO: 5) and 3′ EcoRI-ANP (5′ GAATTCTGAGGAGATTGTAGAGTCACC 3′) (SEQ ID NO: 6). DNA fragment encoding BRL (SEQ ID NO: 2) was amplified by PCR using cDNA which reverse transcribed from Tachypleus tridentatus' RNA as template. Primers 5′ EcoRI-BRL (5′ GAATTCGAAGATGACTGCACGTGACAGAC 3′) (SEQ ID NO: 7) and 3′ NotI-BRL-6His (5′ GCGGCCGCTTAATGATGATGATGATGATGC TTAATTATTATAATAGGTCC 3′) (SEQ ID NO: 8) were used for PCR procedure. Two purified PCR products were digested with NdeI/EcoRI and EcoRI/NotI respectively, ligated with pET23a treated with same restriction enzymes.

The recombinant plasmid was confirmed by sequencing and then transformed to E. coli Top1OF′ and selected on agar plate containing 100 μg/ml Ampicillin. A single colony was picked on the selection plate and grown in 5 ml of Luria-Bertani (LB) medium (1% tryptone, 0.5% yeast extract, and 0.5% sodium chloride) containing the same concentration of the antibiotic at 37° C. overnight for plasmid extraction. The extracted plasmid was then transformed into E. coli expression strain ROSETTA™ (DE3) and selected on agar plate containing 100 μg/ml Ampicillin. A single colony was picked and grown in 1 L LB medium at 37° C. until OD₆₀₀ reached 0.4 to 0.6. Protein expression was induced by addition of IPTG to a final concentration of 0.1 mM and incubation at 16° C. for 16 h. Cells were harvested by centrifugation at 4000×g for 10 min at 4° C., and washed once with PBS. Then, cell pellet was resuspended in 50 mL of equilibrium buffer (20 mM Tris-HCl, 200 mM NaCl, 5 mM imidazole, pH 7.4) supplemented with protease inhibitor (1 mM phenylmethylsulfonyl fluoride, PMSF) and disrupted by a 3 cycles through a cell homogenizer (EMULSIFLEX®-C3 homogenizer) at 15,000 psi. The cell lysate was separated into supernatant and pellet by centrifugation at 16000×g for 30 min at 4° C. to remove cellular debris. The supernatant was subjected to purification by NI SEPHAROSE™ 6 Fast Flow (GE healthcare) column chromatography. The column was first pre-equilibrated with equilibrium buffer and at the end of sample loading, washed with 50 mL equilibrium buffer (W1) and 50 mL wash buffer (20 mM Tris-HCl, 200 mM NaCl, 50 mM imidazole, pH 7.4) (W2). To recover bound protein, the column was eluted with elution buffer (20 mM Tris-HCl, 200 mM NaCl, 300 mM imidazole, pH 7.4). The eluted rBRL was then concentrated and buffer-exchanged to Tris buffer (20 mM Tris-HCl, 200 mM NaCl, pH 7.4).

Results

Expression and Purification of rBRL

rBRL was composed of an artificial N-terminal peptide and a C-terminal horseshoe crab bacteria recognizing lectin (BRL) derived from T. tridentatus. DNA fragments encoding artificial peptide and BRL were separately ligated into pET23a vector and the recombinant plasmid was transformed into E. coli ROSETTA™ (DE3) for protein expression. From 1 L of culture medium, approximately 6 mg of purified rBRL was obtained by Nickel column chromatography, with a recovery rate of 80.6% (FIG. 1). Five-fold higher yield of rBRL than BRL-6His has been achieved; indicating that the artificial peptide fused at the N-terminal end of BRL has successfully facilitated the isolation of rBRL. To further investigate the importance of the artificial peptide in BRL expression, a shorter peptide consisted of first and last 7 amino acids of the peptide were separately fused at the N-terminus of BRL (rBRL(N7) and rBRL(C7), respectively). The expression status revealed that BRL fused with both peptides were expressed in the inclusion body fraction, strongly indicated that full-length artificial peptide was required for soluble rBRL expression (FIGS. 2A and 2B, lane P).

Example 2

Materials and Methods

Reagents

E. coli Top10F′ (Invitrogen) was used for vector construction and DNA manipulation, E. coli expression strain ROSETTA™ (DE3) (Stratagene), vectors pET23a purchased from NOVAGEN® were used for protein expression. All other buffers and reagents are of the highest commercial purity.

Protein Expression and Purification

DNA fragment encoding SEQ ID NO: 1 was amplified by PCR with primers 5′ NdeI-ANP (5′ CATATGTCCAAGCCACTACTACTAC 3′) (SEQ ID NO: 5) and 3′ EcoRI-ANP (5′ GAATTCTGAGGAGATTGTAGAGTCACC 3′) (SEQ ID NO: 6). DNA fragment encoding human eosinophil RNase (SEQ ID NO: 9) was amplified from cDNA which reverse transcribed from asthma patient's RNA. PCR primers 5′ EcoRI-RNase (5′ GAATTCAGACCCCCACAGTTTACGAGG 3′) (SEQ ID NO: 12) and 3′ BamHI-RNase-6His (5′ GGATTCTTAGTGGTGGTGGTGGTGGTGGATGGTGGTATCCAGGTG 3′) (SEQ ID NO: 13) was used for human eosinophil RNase amplification. PCR product encoding SEQ ID NO: 1 and human eosinophil RNase were digested with NdeI/EcoRI and EcoRI/BamHI respectively, ligated with pET23a treated with same restriction enzymes.

The recombinant plasmid was confirmed by sequencing and then transformed to E. coli Top10F′ and selected on agar plate containing 100 μg/ml Ampicillin. A single colony of each clone was picked on the selection plate and grown in 5 ml of Luria-Bertani (LB) medium (1% tryptone, 0.5% yeast extract, and 0.5% sodium chloride) containing the same concentration of the antibiotic at 37° C. overnight for plasmid extraction. The extracted plasmid was then transformed into E. coli expression strain ROSETTA™ (DE3) and selected on agar plate containing 100 μg/ml Ampicillin. A single colony was picked and grown in 1 L LB medium at 37° C. until OD₆₀₀ reached 0.4 to 0.6. Protein expression was induced by addition of IPTG to a final concentration of 0.1 mM and incubation at 16° C. for 16 h. Cells were harvested by centrifugation at 4000×g for 10 min at 4° C., and washed once with PBS. Then, cell pellet was resuspended in buffer A (10 mM sodium phosphate buffer, 1 mM EDTA, pH 7.0) supplemented with protease inhibitor (1 mM phenylmethylsulfonyl fluoride, PMSF) and disrupted by 5 cycles of homogenization at 15,000 psi. After homogenization, the slurry was centrifuged at 16,000×g for 30 min at 4° C. to remove cellular debris. Protein in the supernatant was loaded onto a 5 mL HITRAP™ Heparin HP on a FPLC system (GE Health) with a flow rate of 2 mL/min, washed with buffer A until the OD280 absorbance reached the baseline then proteins were eluted with a linear NaCl gradient (0-2M NaCl). Fractions of each were analyzed by 15% (w/v) SDS-PAGE.

Results

Expression and Purification of reRNase

reRNase was composed of an artificial N-terminal peptide and a C-terminal human eosinophil ribonuclease. DNA fragments encoding artificial peptide and human eosinophil RNase were separately ligated into pET23a vector and the recombinant plasmid was transformed into E. coli ROSETTA™ (DE3) for protein expression. The results showed that reRNase of expected molecular weight of 20.5 kDa was successfully expressed in E. coli BL21 ROSETTA™ (DE3) and most of the overexpressed protein was present in supernatant fraction (FIG. 3A, lane S). The soluble reRNase in supernatant fraction was then purified by HITRAP™ Heparin HP column on FPLC system. FIG. 3A (lane E1 and E2) showed that reRNase could be successfully eluted by a stepwise NaCl gradient. On the other hand, the expression of human eosinophil RNase without an artificial peptide (FIG. 3B) was mainly present in inclusion body (pellet fraction) as previously described.

One skilled in the art readily appreciates that the present invention is well adapted to carry out the objects and obtain the ends and advantages mentioned, as well as those inherent therein. The peptide/recombinant protein, and processes and methods for producing them are representative of preferred embodiments, are exemplary, and are not intended as limitations on the scope of the invention. Modifications therein and other uses will occur to those skilled in the art. These modifications are encompassed within the spirit of the invention and are defined by the scope of the claims.

It will be readily apparent to a person skilled in the art that varying substitutions and modifications may be made to the invention disclosed herein without departing from the scope and spirit of the invention.

All patents and publications mentioned in the specification are indicative of the levels of those of ordinary skill in the art to which the invention pertains. All patents and publications are herein incorporated by reference to the same extent as if each individual publication was specifically and individually indicated to be incorporated by reference.

The invention illustratively described herein suitably may be practiced in the absence of any element or elements, limitation or limitations, which are not specifically disclosed herein. The terms and expressions which have been employed are used as terms of description and not of limitation, and there is no intention that in the use of such terms and expressions of excluding any equivalents of the features shown and described or portions thereof, but it is recognized that various modifications are possible within the scope of the invention claimed. Thus, it should be understood that although the present invention has been specifically disclosed by preferred embodiments and optional features, modification and variation of the concepts herein disclosed may be resorted to by those skilled in the art, and that such modifications and variations are considered to be within the scope of this invention as defined by the appended claims.

Claims

1. An artificial peptide consisting of the amino acid sequence of SEQ ID NO: 1, wherein said peptide can increase solubility of a target fusion protein.

2. A method for increasing expression of a target protein by using the peptide of claim 1, comprising (a) fusing a nucleic acid encoding the peptide of claim 1 with a nucleic acid encoding a target protein to form a recombinant nucleic acid; (b) transforming an expression host cell with the recombinant nucleic acid; and (c) expressing the recombinant nucleic acid in the expression host cell to form a target fusion protein, wherein expression of the target protein is increased.

3. The method of claim 2, wherein the target protein is a glycan binding protein.

4. The method of claim 3, wherein the target protein is a vertebrate plasma lectin.

5. The method of claim 4, wherein the target protein is a bacteria recognizing lectin.

6. The method of claim 3, wherein the target protein is a vertebrate ribonuclease.

7. The method of claim 6, wherein the target protein is a primate eosinophil ribonuclease.

8. The method of claim 6, wherein the target protein is a human eosinophil ribonuclease.

9. The method of claim 2, wherein the expression host cell is a bacterium, a yeast, an insect cell or a mammalian cell.

10. The method of claim 9, wherein the bacterium is Escherichia coli.

11. The method of claim 2, further comprising purifying the target protein.

12. The method of claim 2, wherein the target fusion protein retains the activity of the target protein.